Simultaneous high performance liquid chromatographic (HPLC)‎ determination of ACE inhibitors in pharmaceutical formulations

العناوين الأخرى

الفحص المتزامن للمادة المثبطة HPLC في التحضيرات الصيدلانية بواسطة جهاز ال (ACE-I)‎

مقدم أطروحة جامعية

Dawud, Iyad Rashid

مشرف أطروحة جامعية

Shakya, Ashok Kumar

الجامعة

جامعة عمان الأهلية

الكلية

كلية الصيدلة و العلوم الطبية

القسم الأكاديمي

قسم العلوم الصيدلانية

دولة الجامعة

الأردن

الدرجة العلمية

ماجستير

تاريخ الدرجة العلمية

2013

الملخص الإنجليزي

The purpose of this study was to develop a new high performance liquid chromatographic method for determination of ACE Inhibitors in pharmaceutical formulations.

In the present study a rapid, simple, economical, reverse phase HPLC-PDA method was developed, optimized and validated.

The HPLC method was developed and optimised using Design Expert™ (Version 8.0.6, Stat Ease Inc.

USA) software using central-composite-design, after studying the physicochemical properties.

The Optimised mobile phase was 58 % buffer (0.005M KH2PO4, 0.25ml TEA / L), 25 % acetonitrile and 17 % methanol, final pH was adjusted to 2.80 ± 0.10 using orthophosphoric acid.

The flow rate was 1.0 ml / min.

The signals were monitored using PDA detector (set between λ 200-400 nm).

Quantitation was carried out at 215 nm.

The run time was less than 8 minutes.

The linearity of the developed method was ranged from 5-35 μg / ml for different drugs.

LOD were 0.232, 0.345, 0.476, 0.026, 0.280, 0.609, and 0.141 μg / ml for lisinopril, hydrochlorothiazide (HCT), captopril, imidapril, indapamide, perindopril and trandolapril respectively.

Whereas LOQ were 0.702, 1.044, 1.443, 0.079, 0.848, 1.846 and 0.428 μg / ml for lisinopril, HCT, captopril, imidapril, indapamide, perindopril and trandolapril respectively.

The intra- and inter-day precision (coefficient of variation) of the method was less than 2 %, which indicates highly precise result during the study.

The accuracy of the method were ranged from 102.4-106.6, 99.5-103.5, 102.9-104.3, 97.0¬99.0, 97.6-98.8, 97.0-99.6 and 97.0-98.6 % for lisinopril, HCT, captopril, imidapril, indapamide, perindopril, and trandolapril respectively.

In conclusion this method presented here is sensitive, rapid, accurate, precise, economic, robust, rugged and selective for the routine analysis of the drug in formulation and raw material without changing the chromatographic parameters for these drugs.

التخصصات الرئيسية

علم الصيدلة

الموضوعات

• الإنزيم المحول للأنجيوتنسين

• APA
• MLA
• AMA

لغة النص

الإنجليزية

نوع البيانات

رسائل جامعية

رقم السجل

BIM-357940